GMP involves manufacturing the products in a way to get quality products while following the Guidelines. The guidelines related to good manufacturing practices will be updated regularly in this section.
- Usage of Expired Raw Materials to Manufacture Drug
- Site Acceptance Test (SAT)
- 3 Types of Airlocks and its Purpose and applications
- Granulation Technique in tablet manufacturing
- Deviation, Types of Deviations in Pharmaceuticals
- Change Control in Pharma, Classification: What it is?
- WHO-GMP Document Check List for Visitors
- Role of IPQA during Line Clearance
- Lean Six Sigma in Pharmaceuticals
- What is GMP | cGMP | GMP Principle
- Contamination and Cross-contamination in Manufacturing
- Difference between Static and Dynamic Pass box
- Good Documentation Practice (GDP) in pharmaceuticals
- GxP in Pharmaceuticals industries (FDA guidelines)
- Difference between Validation, Calibration, and Qualification in Pharma
- CAPA Corrective and preventive action in Pharmaceutical
- Handling of Laboratory Incident in Pharma
- SOP on Storage and Hold time study for Products
- Factory Acceptance Test (FAT) in Pharmaceutical
- Lux or Light intensity standards in pharma industry
- Stainless Steel Types in Pharmaceutical (Detailed Study)
- Line Clearance Checklist point production/packing
